myPrenatal

Non-invasive and above all comprehensive prenatal testing

What is myPrenatal?

It is a state-of-the-art prenatal screening test that allows to study the most common chromosomal abnormalities: Down syndrome, Edwards, Patau, and sex chromosome alterations.

This test analyzes free fetal DNA using cutting-edge technology, providing higher reliability and more information compared to alternative prenatal screening tests.

Why choose myPrenatal

Comprehensive

Assesses the risk of serious diseases that may affect your newborn’s health.

Easy and safe

No risk for your baby, only a maternal blood sample will be needed.

Precise

Eliminates unnecessary invasive procedures, increasing accuracy over combined screening.

Fast

Results in 5 business days.

Quality

The test is performed in our laboratories in Europe by a team that has extensive experience and is CE-IVD marked.

Intended users

myPrenatal can be performed by any pregnant woman from the 10th week of pregnancy.

It can be performed for both singleton and twin pregnancies.

Suitable for pregnancies involving assisted reproduction, even for gamete donation.

myPrenatal GenomeScreen

With the additional service myPrenatal GenomeScreen you can broaden your results by performing a more comprehensive screening including:

Genetic alterations affecting only part of a chromosome

Fetal DNA is analyzed to find loss or gain of large DNA segments that can lead to disorders such as delayed cognitive development.

Alterations in chromosome total number

This option allows to broaden the analysis to the rest of the fetal chromosomes, thereby including those infrequent alterations in the number of chromosomes, mostly related to fetal loss or other structural abnormalities.

in only takes 15 minutes